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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37337생성일: 2026년 10월 23일

Sodium Hydroxide → (2S,4S)-4-(4-methoxybenzyl)thio-1-(4-nitrobenzyloxycarbonyl)-L-proline

https://huagongshe.com/ko/reaction/37337

반응식

참여 물질

역할이름HCID투입량
반응물Sodium HydroxideHCID 14798—
반응물4-Nitrobenzyl chloroformateHCID 78205—
반응물(4S)-4-{[(4-Methoxyphenyl)methyl]sulfanyl}-L-prolineHCID 15297070—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(2S,4S)-4-(4-methoxybenzyl)thio-1-(4-nitrobenzyloxycarbonyl)-L-prolineHCID 1529707177.5%

반응 단계

1.87 g of (2S,4S)-4-(4-methoxybenzylthio)-2-pyrrolidinecarboxylic acid [prepared as described in step (a) above] was suspended in 80 ml of a 1:1 by volume mixture of tetrahydrofuran and water. This suspension was then converted to a homogeneous solution by the addition of 7 ml of a 1N aqueous solution of sodium hydroxide. Whilst stirring this solution on an ice bath, 10 ml of a tetrahydrofuran solution containing 1510 mg of 4-nitrobenzyloxycarbonyl chloride and 7 ml of a 1N aqueous solution of sodium hydroxide were gradually added dropwise at the same time, and the resulting mixture was stirred under the same conditions for 10 minutes. At the end of this time, the tetrahydrofuran was removed by evaporation under reduced pressure. 1N aqueous hydrochloric acid was added to the reaction solution to adjust its pH to a value of between 2 and 3. The crystals which separated were collected by filtration, washed well with water and dried in the air. They were then further washed with a small amount of diethyl ether and dried, to obtain 2.42 g of the title compound, melting at 96°-98° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420119
출처 데이터셋uspto-grants-1995_05
ORD IDord-95f2d28d048d4aed86abf3b0f36ff58c
출처 메모uspto-grants-1995_05